autosomal recessive ataxia
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2021 ◽  
Vol 23 (1) ◽  
pp. 153-160
Author(s):  
Sara Uccella ◽  
Livia Pisciotta ◽  
Mariasavina Severino ◽  
Enrico Bertini ◽  
Thea Giacomini ◽  
...  

Author(s):  
Е.П. Нужный ◽  
Н.Ю. Абрамычева ◽  
Е.Г. Воробьева ◽  
Е.О. Иванова ◽  
Ю.А. Шпилюкова ◽  
...  

Синдром CANVAS (мозжечковая атаксия, невропатия и вестибулярная арефлексия) - аутосомно-рецессивная атаксия с поздним дебютом, обусловленная носительством биаллельной экспансии (AAGGG)n во 2-м интроне гена RFC1. До настоящего момента отсутствуют сведения о распространенности данного заболевания в российских семьях. Нами был проведен поиск биаллельной экспансии AAGGG-повторов у 35 российских пациентов с поздней мозжечковой атаксией. Верифицированы 5 пациентов (14,3%) с синдромом CANVAS и характерной клинической картиной. CANVAS (cerebellar ataxia, neuropathy and vestibular areflexia) is a late-onset autosomal recessive ataxia due to biallelic (AAGGG)n repeat expansion in the 2nd intron of the RFC1 gene. There is no information on the CANVAS prevalence in Russian families. We searched for biallelic expansion of AAGGG repeats in 35 Russian patients with late-onset cerebellar ataxia. Five patients (14.3%) with CANVAS syndrome and a characteristic clinical picture were verified.


2019 ◽  
Vol 63 ◽  
pp. 66-72 ◽  
Author(s):  
Edoardo Monfrini ◽  
Letizia Straniero ◽  
Sara Bonato ◽  
Giacomo Monzio Compagnoni ◽  
Andreina Bordoni ◽  
...  

2019 ◽  
Vol 119 (9) ◽  
pp. 74
Author(s):  
E. P. Nuzhnyi ◽  
N. Yu. Abramycheva ◽  
S. A. Klyushnikov ◽  
Yu. A. Seliverstov ◽  
A. S. Vetchinova ◽  
...  

2017 ◽  
Vol 18 (1) ◽  
pp. 52-56
Author(s):  
Tahira N Choudry ◽  
David Hilton-Jones ◽  
Graham Lennox ◽  
Henry Houlden

A 23-year-old woman had presented initially to a podiatrist complaining of poorly fitting shoes during her adolescence. After extensive neurological review, she was diagnosed with ataxia with oculomotor apraxia type 2. This is a progressive autosomal recessive ataxia associated with cerebellar atrophy, peripheral neuropathy and an elevated serum α-fetoprotein. Within Europe, it is the most frequent autosomal recessive ataxia after Friedreich’s ataxia and is due to mutations in the senataxin (SETX) gene. The age of onset is approximately 15 years.The diagnosis of oculomotor apraxia type 2 is often challenging. We provide a framework for assessing a young ataxic patient with or without oculomotor apraxia and review clues that will aid diagnosis. The prognosis, level of disability, cancer and immunosuppression risk all markedly differ between the conditions. Patients and their families need the correct diagnosis for genetic counselling, management and long-term surveillance with appropriate subspecialty services.


2016 ◽  
Vol 31 (11) ◽  
pp. 1754-1756 ◽  
Author(s):  
Maria Thereza Drumond Gama ◽  
Gabrielle Houle ◽  
Anne Noreau ◽  
Alexandre Dionne-Laporte ◽  
Patrick A. Dion ◽  
...  

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